Effect of M2-macrophage treated lymphatic endothelial cells on angiogenesis that promoted osteointegration.

Early vascularization plays an essential role during the whole process in bone regeneration because of the function of secreting cytokines, transporting nutrients and metabolic wastes. As the preliminary basis of bone repair, angiogenesis is regulated by immune cells represented by macrophages to a great extent. However, with the discovery of the endolymphatic circulation system inside bone tissue, the role of vascularization became complicated and confusing. Herein, we developed a macrophage/lymphatic endothelial cells (LECs)/human umbilical vein endothelial cells (HUVECs) co-culture system to evaluate the effect of macrophage treated lymphatic endothelial cells on angiogenesis in vitro and in vivo. In this study, we collected the medium from macrophage (CM) for LECs culture. We found that CM2 could promote the expression of LECs markers and migration ability, which indicated the enhanced lymphogenesis. In addition, the medium from LECs was collected for culturing HUVECs. The CM2-treated LECs showed superior angiogenesis property including the migration capacity and expression of angiogenetic markers, which suggested the superior vascularization. Rat femoral condyle defect model was applied to confirm the hypothesis in vivo. Generally, M2-macrophage treated LECs showed prominent angiogenetic potential coupling with osteogenesis.

Facilitating the Electrochemical Oxidation of ZnS through Iodide Catalysis for Aqueous Zinc-Sulfur Batteries.

Aqueous zinc-sulfur (Zn-S) batteries show great potential for unlocking high energy and safety aqueous batteries. Yet, the sluggish kinetic and poor redox reversibility of the sulfur conversion reaction in aqueous solution challenge the development of Zn-S batteries. Here, we fabricate a high-performance Zn-S battery using highly water-soluble ZnI2 as an effective catalyst. In situ experimental characterizations and theoretical calculations reveal that the strong interaction between I- and the ZnS nanoparticles (discharge product) leads to the atomic rearrangement of ZnS, weakening the Zn-S bonding, and thus facilitating the electrochemical oxidation reaction of ZnS to S. The aqueous Zn-S battery exhibited a high energy density of 742 Wh kg(sulfur) -1 at the power density of 210.8 W kg(sulfur) -1 and good cycling stability over 550 cycles. Our findings provide new insights about the iodide catalytic effect for cathode conversion reaction in Zn-S batteries, which is conducive to promoting the future development of high-performance aqueous batteries.

Diatomic Catalysts for Aqueous Zinc-Iodine Batteries: Mechanistic Insights and Design Strategies.

There has been a growing interest in developing catalysts to enable the reversible iodine conversion reaction for high-performance aqueous zinc-iodine batteries (AZIBs). While diatomic catalysts (DACs) have demonstrated superior performance in various catalytic reactions due to their ability to facilitate synergistic charge interactions, their application in AZIBs remains unexplored. Herein, we present, for the first time, a DAC comprising Mn-Zn dual atoms anchored on a nitrogen-doped carbon matrix (MnZn-NC) for iodine loading, resulting in a high-performance AZIB with a capacity of 224 mAh g-1 at 1 A g-1 and remarkable cycling stability over 320,000 cycles. The electron hopping along the Mn-N-Zn bridge is stimulated via a spin exchange mechanism. This process broadens the Mn 3dxy band width and enhances the metallic character of the catalyst, thus facilitating charge transfer between the catalysts and reaction intermediates. Additionally, the increased electron occupancy within the d-orbital of Zn elevates Zn's d-band center, thereby enhancing chemical interactions between MnZn-NC and I-based species. Furthermore, our mechanism demonstrates potential applicability to other Metal-Zn-NC DACs with spin-polarized atoms. Our work elucidates a clear mechanistic understanding of diatomic catalysts and provides new insights into catalyst design for AZIBs.

Thyroid dysfunction and sarcopenia: a two-sample Mendelian randomization study.

Objective: Observational studies have shown positive associations between thyroid dysfunction and risk of sarcopenia. However, the causality of this association remains unknown. This study aimed to evaluate the potential causal relationship between thyroid dysfunction and sarcopenia using Mendelian randomization (MR). Methods: This study collected pooled data from genome-wide association studies focusing on thyroid dysfunction and three sarcopenia-related features: low hand grip strength, appendicular lean mass (ALM), and walking pace, all in individuals of European ancestry. The primary analytical method used was inverse-variance weighted, with weighted median and MR-Egger serving as complementary methods to assess causal effects. Heterogeneity and pleiotropy tests were also performed, and the stability of the results was evaluated using the Leave-one-out. Results: The MR analysis indicated that hyperthyroidism could lead to a significant decrease in ALM in the extremities (OR = 1.03; 95% CI = 1.02 to 1.05; P < 0.001). The analysis also found that hypothyroidism could cause a notable reduction in grip strength (OR = 2.03; 95% CI = 1.37 to 3.01; P < 0.001) and walking pace (OR = 0.83; 95% CI = 0.77 to 0.90; P < 0.001). There was a significant association between subclinical hyperthyroidism and a reduced walking pace (OR = 1.00; 95% CI = 0.99 to 1.00; P = 0.041). Conclusion: This study provides evidence that hyperthyroidism, hypothyroidism, and subclinical hyperthyroidism can all increase the risk of sarcopenia.

A salt-concentrated electrolyte for aqueous ammonium-ion hybrid batteries.

The development of aqueous ammonium-ion batteries (AAIBs) is currently attracting great attention because of the interesting electrochemical features induced by the charge carrier NH4+. One possible way to improve the performance of AAIBs is increasing the salt concentration in the electrolyte. Yet, few studies focus on the complex electrode-electrolyte interface behaviors in highly concentrated electrolytes, which affect the electrochemical performance of AAIBs significantly. Herein, we aim to understand the impact of CH3COONH4 electrolyte concentration on the NH4+ storage performance of a bimetallic hydroxide material. Experimental and theoretical simulation results indicate that the acetate anion will participate in the construction of the solvated NH4+ in a highly concentrated electrolyte, facilitating the adsorption of the solvated NH4+ cluster on the electrode surface. Besides, a new partial de-solvation model is also proposed, demonstrating an energy favorable de-solvation process. Finally, an ammonium-ion hybrid battery is designed, which provides a high average discharge voltage of 1.7 V and good energy density of 368 W h kg(cathode)-1, outperforming most of the state-of-the-art aqueous batteries. This work provides new understanding about the electrode's interfacial chemistry in different concentrated CH3COONH4 electrolytes, establishes a correlation between the electrolyte concentration and the electrode's performances, and demonstrates the superiority of the hybrid ammonium-ion battery design.

Influence of Shielding Gas on Microstructure and Properties of GMAW DSS2205 Welded Joints.

In the present study, the microstructures and properties of DSS 2205 solid wire MIG welded samples prepared in different shielding gases (pure Ar gas, 98%Ar + 2%O2 and 98%Ar + 2%N2) were investigated for improving the weldability of DSS 2205 welded joint. The work was conducted by mechanical property tests (hardness and tensile test) and corrosion resistance property tests (immersion and electrochemical tests). The results show that adding 2%O2 into pure Ar gas as the shielding gas decreases crystal defects (faults) and improves the mechanical properties and corrosion resistance of the welded joints. Phase equilibrium and microstructural homogeneity in welded seam (WS) and heat-affected zone (HAZ) can be adjusted and the strength and corrosion resistance of welded joints increased obviously by adding 2%N2 to pure Ar gas as the shielding gas. Compared with DSS 2205 solid wire MIG welding in 98%Ar + 2%O2 mixed atmosphere, the strength and corrosion resistance of welded joints are improved more obviously in 98%Ar + 2%N2 mixed atmosphere.

A 3D free-standing Co doped Ni2P nanowire oxygen electrode for stable and long-life lithium-oxygen batteries.

Exploring oxygen electrodes with superior bifunctional catalytic activity and suitable architecture is an effective strategy to improve the performance of lithium-oxygen (Li-O2) batteries. Herein, the internal electronic structure of Ni2P is regulated by heteroatom Co doping to improve its catalytic activity for oxygen redox reactions. Meanwhile, magnetron sputtering N-doped carbon cloth (N-CC) is used as a scaffold to enhance the electrical conductivity. The deliberately designed Co-Ni2P on N-CC (Co-Ni2P@N-CC) with a typical 3D interconnected architecture facilitates the formation of abundant solid-liquid-gas three-phase reaction interfaces inside the architecture. Furthermore, the rational catalyst/substrate interfacial interaction is capable of inducing a solvation-mediated pathway to form toroidal-Li2O2. The results show that the Co-Ni2P@N-CC based Li-O2 battery exhibits an ultra-low overpotential (0.73 V), enhanced rate performance (4487 mA h g-1 at 500 mA g-1) and durability (stable operation over 671 h). The pouch-type battery based on the Co-Ni2P@N-CC flexible electrode runs stably for 581 min in air without obvious voltage attenuation. This work verifies that heterogeneous atom doping and interface interaction can remarkably strengthen the performance of Li-O2 cells and thus pave new avenues towards developing high-performance metal-air batteries.

Configuration of gradient-porous ultrathin FeCo2S4 nanosheets vertically aligned on Ni foam as a noncarbonaceous freestanding oxygen electrode for lithium-oxygen batteries.

The degradation of oxygen electrodes caused by oxygen species in lithium-oxygen (Li-O2) batteries deteriorates their energy efficiency and cyclability and seriously hinders their commercial application. To achieve high energy efficiency and long-term cycle life, gradient-porous ultrathin FeCo2S4 nanosheets on Ni foam (FeCo2S4@Ni) were deliberately designed as a noncarbonaceous freestanding oxygen electrode for Li-O2 batteries. Notably, the gradient-porous structure in FeCo2S4@Ni can offer sufficient active sites as well as mitigate polarization caused by the mass transfer during discharge and charge. The synergistic effect of the two transition metals, Fe2+ and Co3+, optimizes their d-band electronic structure and enhances the intrinsic activity of the oxygen electrode. Benefiting from the above merits, the FeCo2S4@Ni based Li-O2 battery demonstrates greatly increased discharge capacity (8001 mA h g-1), improved rate capability (with a high capacity of 4401 mA h g-1 at 500 mA g-1), and enhanced cycling stability (with a low overpotential of below 1 V after 109 cycles). Our work demonstrates that the battery performance can be improved by regulating the structure and composition of the oxygen electrode and provides a promising strategy for developing high performance Li-O2 batteries.

Impacts of Stress Relief Treatments on Microstructure, Mechanical and Corrosion Properties of Metal Active-Gas Welding Joint of 2205 Duplex Stainless Steel.

Stress relief treatments were carried out separately with a pneumatic chipping hammer, ultrasonic peening treatment, and heat treatment for metal active-gas welding (MAG) welded joints of 2205 duplex stainless steel. The effects of these methods on the residual stress, microstructure, mechanical properties and corrosion resistance of welded joints were studied. Results show the stress state of the weld and the surrounding area was effectively improved by the pneumatic chipping hammer and ultrasonic peening treatment, and the residual stress field of the surface layer changed from tensile stress to compressive stress. On the contrary, low-temperature stress relieving annealing had no obvious effect on stress distribution. After the pneumatic chipping hammer and ultrasonic peening treatment, the welded joints were machined and hardened. Correspondingly, strength and hardness were improved. However, the heat treatment only led to a slight decrease in strength and hardness due to the static recovery of the welded joint structure. All stress relief methods effectively improved the corrosion resistance of welded joints, with the ultrasonic peening treatment giving the best performance.

In Situ Fabricating Oxygen Vacancy-Rich TiO2 Nanoparticles via Utilizing Thermodynamically Metastable Ti Atoms on Ti3C2Tx MXene Nanosheet Surface To Boost Electrocatalytic Activity for High-Performance Li-O2 Batteries.

Catalysts with high performance are urgently needed in order to accelerate the reaction kinetics of the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in lithium-oxygen (Li-O2) batteries. Herein, utilizing thermodynamically metastable Ti atoms on the Ti3C2Tx MXene nanosheet surface as the nucleation site, oxygen vacancy-rich TiO2 nanoparticles were in situ fabricated on Ti3C2Tx nanosheets (V-TiO2/Ti3C2Tx) and used as the oxygen electrode of Li-O2 batteries. Oxygen vacancy (Vo) can boost the migration rate of electrons and Li+ as well as act as the active sites for catalyzing the ORR and OER. Based on the above merits, V-TiO2/Ti3C2Tx-based Li-O2 battery shows improved performance including the ultralow overpotential of 0.21 V, high specific capacity of 11 487 mA h g-1 at a current density of 100 mA g-1, and excellent round-trip efficiency (93%). This work proposes an effective strategy for researching high-performance oxygen electrodes for Li-O2 batteries via introducing Vo-rich oxides on two-dimensional MXene.